Evidence map›Paper›PMID 28405705›Full record

ArticleDer Urologe. Ausg. A2017

[Cost effectiveness of GnRH antagonists in patients with prostate cancer and cardiovascular risk : Comparative analysis against Leuprorelin by the Number Needed to Treat].

D Anderson, J Lehmann, T Ecker, S Vosgerau, V Donatz

Erratum issuedOpen access · hybridAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Der Urologe. Ausg. A, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

D AndersonEcker + Ecker GmbH, Warburgstraße 50, 20354, Hamburg, Deutschland. d.anderson@gmx.de.
J LehmannKlinik für Urologie, Städtisches Krankenhaus, Kiel, Deutschland.
T EckerEcker + Ecker GmbH, Warburgstraße 50, 20354, Hamburg, Deutschland.
S VosgerauFerring Arzneimittel GmbH, Kiel, Deutschland.
V DonatzFerring Arzneimittel GmbH, Kiel, Deutschland.
Ferring Pharmaceuticals (Germany) · DESchmerzklinik Kiel · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies suggest that androgen deprivation therapy (ADT) is associated with increased cardiovascular (CV) risk for patients with hormone-sensitive prostate cancer (PCa) and pre-existing CV disease. This risk seems to be different for the gonadotropin-releasing hormone (GnRH) agonists leuprolide and goserelin and GnRH antagonists, whereas the slightly more expensive GnRH antagonist shows a beneficial risk profile. The present study assesses the cost effectiveness of degarelix compared to leuprolide for PCa patients with increased CV risk.

methodsThis analysis is based on a pooled analysis of six phase III, randomized, controlled trials comparing the GnRH agonists leuprolide and goserelin with the GnRH antagonist degarelix. For the combined endpoint of CV events or death a superiority of degarelix was determined with a Number-Needed-to-Treat of 12. From the perspective of German statutory health insurance, this evaluation estimates and compares the additional drug costs of degarelix treatment to the cost of one (avoided) CV event. The CV event costs were estimated via emergency treatment and transportation, inpatient treatment, and rehabilitation. The difference of these two cost pools divided by 12 yields the average saving per patient and year.

resultsFor every 12 PCa patients with CV history that are treated with GnRH antagonists to prevent one CV event, there will be additional drug costs in comparison with leuprolide treatment of € 3111 per year. Costs of € 8447 per year are prevented. Therefore, each patient with a history of CV who is treated with degarelix instead of a leuprolide generates savings of € 445 per patient and year.

conclusionsCompared to leuprolide, degarelix is cost effective for patients with increased CV risk.

Indexed as

Antineoplastic Agents, HormonalCardiovascular DiseasesCost-Benefit AnalysisGonadotropin-Releasing HormoneHumansLeuprolideMaleMeta-Analysis as TopicOligopeptidesProstatic NeoplasmsRandomized Controlled Trials as TopicRisk Factorsacetyl-2-naphthylalanyl-3-chlorophenylalanyl-1-oxohexadecyl-seryl-4-aminophenylalanyl(hydroorotyl)-4-aminophenylalanyl(carbamoyl)-leucyl-ILys-prolyl-alaninamideAntineoplastic Agents, HormonalGonadotropin-Releasing HormoneLeuprolideOligopeptidesAndrogen deprivation therapyCost-effectiveness analysisDegarelixNumbers needed to treatProstate cancer

Identifiers

PMID28405705
OpenAlexW2605932937

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.